Canonical Allele Identifier:
CA1439212926
Gene:
Linked Data
dbSNP Id:
rs1486904125
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578287G>C , CM000666.2:g.12578287G>C | GRCh38 |
| NC_000004.11:g.12579911G>C , CM000666.1:g.12579911G>C | GRCh37 |
| NC_000004.10:g.12189009G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925406.1:n.106+31055C>G | ||
| XR_001741374.1:n.254+44368C>G | ||
| XR_925406.3:n.140+31055C>G |